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Course of Multimodal Therapy and Genetic Profile of Hereditary Leiomyomatosis...

Masuda(H),Sato(T),Sato(S),Goto(T),Katayama... Urol Int 2026-00-00

...FH) gene. Here, we report a case of HLRCC with early recurrence during adjuvant therapy following radical nephrectomy. A...

Financing and health system capacity for precision medicine in Asia: a six co...

Peh(ALT),Teerawattananon(Y),Yuen(JXY),Char... Health Aff Sch 2026-09-00

...FH] cascade testing), next-generation sequencing (NGS) applications (rare diseases, oncology, pharmacogenomics), and AI-...

Unveiling the dual roles of chromium in mediating vanadium sequestration by f...

Zhou(D),Tang(Y),Chen(Y),Huang(Z),Sun(J),Ch... Water Res 2026-09-06

...Fh) transformation experiments, spectroscopic characterization, electron microscopy, and density functional theory calcu...

Pathology-Driven Diagnosis of Hereditary Leiomyomatosis and Renal Cell Carcin...

Uchiyama(T),Okazaki(S),Ando(S),Takeda(M),M... IJU Case Rep 2026-09-00

...FH)-deficient renal cell carcinoma (RCC). Although 200-300 families have been identified worldwide, its true prevalence ...

A Case of a Fumarate Hydratase Deficient Astrocytoma in Association With a Ge...

Alfattal(R),Nagarajan(P),O'Brien(B),Quezad... Am J Surg Pathol 2026-01-01

...FH-deficient leiomyomas, a retrospective analysis of his brain tumor revealed FH deficiency and a germline FH alteration...

Adult Mixed Epithelial and Stromal Tumor of the Kidney Harbors Recurrent Whol...

Coiner(BL),Bayrak(BY),Isikci(OT),Siegmund(... Am J Surg Pathol 2026-09-17

...FH, SDHA/B/D, ELOC, TFEB, TFE3, DICER1, MET, MTOR, and TSC1/2). Of 13 cases with follow-up (median: 81.2 mo), no recurre...

Comprehensive Germline Profiling of High-Grade Serous Ovarian Cancer Using Wh...

Cho(HL),Bak(SE),Han(MR),Choi(YJ) Int J Mol Sci 2026-06-19

...FH, and 33.3% without. The HGSOC group and controls with FH exhibited similar P/LP germline mutation patterns in ovarian...

Genetic Influence on LDL-Cholesterol Levels: Role of Polygenic Risk Scores an...

Ferrandino(M),Cerrato(Y),Iannuzzo(G),Calca... Genes (Basel) 2026-06-21

...FH) is the most common monogenic disorder, caused by rare high-impact variants in genes involved in LDL uptake. Other mo...

Dyslipidemia and Retinal Microvascular Health in Children and Adolescents: A ...

Xhafa(K),Groselj(U) Children (Basel) 2026-06-17

...FH) had lower capillary densities and larger foveal avascular zone areas detected by optical coherence tomography angiog...

Research on Covert Communication in Satellite-Ground-Integrated Sensor Networ...

Ni(L),Cai(Y),Li(X),Hu(H),Chu(Z),Qi(Y) Sensors (Basel) 2026-06-11

...FH-DL-MPWFRFT) is proposed from the perspective of physical layer security. The proposed scheme integrates the constella...

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